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SENSUS

NeuroMetrix, Inc. · Model SE-SK2 · UDI-DI 00851221006285

NUH Prescription
10
510(k) clearances
119
Adverse events
0
Recalls
171
Facilities

Description

SENSUS System Kit, 1 Device (Includes 1 SE-S01 or QE-P01)

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.